Protocol for stratification of triple-negative breast cancer patients using in silico signaling dynamics
Personalized kinetic models can predict potential biomarkers and drug targets. Here, we provide a step-by-step approach for building an executable mathematical model from text and integrating transcriptomic datasets. We additionally describe the steps to personalize the mechanistic model and to stra...
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Veröffentlicht in: | STAR protocols 2022-09, Vol.3 (3), p.101619-101619, Article 101619 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Personalized kinetic models can predict potential biomarkers and drug targets. Here, we provide a step-by-step approach for building an executable mathematical model from text and integrating transcriptomic datasets. We additionally describe the steps to personalize the mechanistic model and to stratify patients with triple-negative breast cancer (TNBC) based on in silico signaling dynamics. This protocol can also be applied to any signaling pathway for patient-specific modeling.
For complete details on the use and execution of this protocol, please refer to Imoto et al. (2022).
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•A computational framework for patient-specific modeling•Integration of clinical data and cell line data for model calibration•Building a mechanistic dynamic model from .txt file•Stratification of patients with breast cancer based on in silico signaling dynamics
Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
Personalized kinetic models can predict potential biomarkers and drug targets. Here, we provide a step-by-step approach for building an executable mathematical model from text and integrating transcriptomic datasets. We additionally describe the steps to personalize the mechanistic model and to stratify patients with triple-negative breast cancer (TNBC) based on in silico signaling dynamics. This protocol can also be applied to any signaling pathway for patient-specific modeling. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2022.101619 |